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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14092
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dc.contributor.authorPant, Debi D.-
dc.date.accessioned2024-02-07T11:08:46Z-
dc.date.available2024-02-07T11:08:46Z-
dc.date.issued2013-03-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0167732212004370-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14092-
dc.description.abstractElectronic absorption and fluorescence spectra of protonated 6-methoxyquinoline (6MQ+) and neutral 6-methoxyquinoline (6MQ) have been recorded at room temperature in wide range of solvents of different polarities. The absorption maximum remains almost unchanged with the increase in solvent polarity, whereas a red shift in fluorescence emission maximum was observed. The ground-state dipole moment and the first excited singlet state dipole moment of 6MQ+ and 6MQ were obtained from Bakhshiev's and Bilot–Kawski's equations by means of solvatochromic shift method. High values of dipole moment are observed for excited state as compared to the corresponding ground state dipole moment values of 6MQ+ and 6MQ and this is attributed to the more polar excited states of 6MQ+ and 6MQ.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPhysicsen_US
dc.subjectSolvatochromic shiften_US
dc.subjectDipole momenten_US
dc.subjectDipole momenten_US
dc.subjectAbsorptionen_US
dc.titleSolvatochromatic shift of absorption and fluorescence spectra of 6-methoxyquinoline: Estimation of ground and excited state dipole momentsen_US
dc.typeArticleen_US
Appears in Collections:Department of Physics

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